ENST00000252288.8:c.526G=
MANE Select
|
ENSP00000252288.1:p.Glu176=
|
|
ENST00000447102.8:c.526G=
|
ENSP00000403536.2:p.Glu176=
|
|
ENST00000591788.3:c.209G=
|
|
|
ENST00000640164.1:n.359G=
|
|
|
ENST00000640762.1:c.457G=
|
ENSP00000492031.1:p.Glu153=
|
|
ENST00000252288.6:c.526G=
|
ENSP00000252288.1:p.Glu176=
|
|
ENST00000447102.7:c.526G=
|
ENSP00000403536.2:p.Glu176=
|
|
ENST00000591788.2:c.211G=
|
ENSP00000466341.2:p.Glu71=
|
|
NM_000156.5:c.526G=
|
NP_000147.1:p.Glu176=
|
|
NM_138924.2:c.526G=
|
NP_620279.1:p.Glu176=
|
|
NM_000156.6:c.526G=
MANE Select
|
NP_000147.1:p.Glu176=
|
|
NM_138924.3:c.526G=
|
NP_620279.1:p.Glu176=
|
|